Data / Medical devices / Germany / Invidia Medical GMBH U Co KG
Invidia Medical GMBH U Co KG: FDA-registered device maker in Emmingen-Liptingen Baden-Wurttemberg, Germany, 4 510(k) clearances
Invidia Medical GMBH U Co KG is registered with the FDA (registration 3010399422) in Emmingen-Liptingen Baden-Wurttemberg, Germany. It lists 74 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 8, 2018. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3010399422
- Address
- Carl-Benz-Str. 28, Emmingen-Liptingen Baden-Wurttemberg, Germany, 78576
- Owner or operator
- INVIDIA Medical GmbH u CO KG (10046503)
- Roles
- Repackager or relabeler
- First device listed
- March 31, 2014
- Registered through
- 2027
- Brand names listed
- Laparoscope, General and Plastic Surgery, Luer-Lock tube connector, Luer-lock tube connector with stopcock, PREMIUM UHD 4K ARTHRO/SINUSCOPE 175MM/70 /4MM
Devices it lists
| Device | Product code | Class | Role | Source |
|---|
| Accessories, Arthroscopic | NBH | 1 | Repackager or relabeler | accessdata.fda.gov |
| Accessories, Photographic, For Endoscope (Exclude Light Sources) | FEM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Airway Suction Kit | OFO | 1 | Repackager or relabeler | accessdata.fda.gov |
| Applier, Surgical, Clip | GDO | 1 | Repackager or relabeler | accessdata.fda.gov |
| Arthroscope | HRX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Blade, Saw, General & Plastic Surgery, Surgical | GFA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Caliper, Ophthalmic | HOE | 1 | Repackager or relabeler | accessdata.fda.gov |
| Camera, Television, Endoscopic, Without Audio | FWF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Camera, Television, Surgical, Without Audio | FWB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cart, Emergency, Cardiopulmonary (Excluding Equipment) | BZN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Clamp | HXD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Clamp, Penile | FHA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Clamp, Surgical, General & Plastic Surgery | GDJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Container, Specimen, Non-Sterile | NNI | 1 | Repackager or relabeler | accessdata.fda.gov |
| Curette | HTF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Curette, Adenoid | KBJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Curette, Ophthalmic | HNZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cystoscope And Accessories, Flexible/Rigid | FAJ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Depressor, Metal Tongue, Surgical | KBL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Dilator, Cervical, Fixed Size | HDQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Dilator, Rectal | FFP | 1 | Repackager or relabeler | accessdata.fda.gov |
| Dislodger, Stone, Basket, Ureteral, Metal | FFL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Electrode, Electrosurgical, Active, Urological | FAS | 2 | Repackager or relabeler | accessdata.fda.gov |
| Elevator | HTE | 1 | Repackager or relabeler | accessdata.fda.gov |
| Elevator, Ent | KAD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Forceps, Biopsy, Gynecological | HFB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Forceps, General & Plastic Surgery | GEN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Forceps, Ophthalmic | HNR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Forceps, Rongeur, Surgical | EMH | 1 | Repackager or relabeler | accessdata.fda.gov |
| Fork, Tuning | GWX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Gag, Mouth | KBN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Guide, Needle, Surgical | GDF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hammer, Surgical | FZY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Handle, Scalpel | GDZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hemostat | HRQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Holder, Needle; Orthopedic | HXK | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hook, Ophthalmic | HNQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hook, Surgical, General & Plastic Surgery | GDG | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hysteroscope (And Accessories) | HIH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Hysteroscope Accessories | NWW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Knife, Amputation | GDN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Knife, Ent | KTG | 1 | Repackager or relabeler | accessdata.fda.gov |
| Knife, Ophthalmic | HNN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Knife, Surgical | EMF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Led Light Source | NTN | 2 | Repackager or relabeler | accessdata.fda.gov |
| Light Source, Endoscope, Xenon Arc | GCT | 2 | Repackager or relabeler | accessdata.fda.gov |
| Light, Fiber Optic, Dental | EAY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Lithotriptor, Biliary Mechanical | LQC | 2 | Repackager or relabeler | accessdata.fda.gov |
| Mirror, Mouth | EAX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Osteotome, Manual | GFI | 1 | Repackager or relabeler | accessdata.fda.gov |
| Otoscope | ERA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Probe | HXB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Probe, Lachrymal | HNL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Rasp, Nasal | KBA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Rasp, Surgical, General & Plastic Surgery | GAC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Retractor | GAD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Retractor, Self-Retaining | FFO | 1 | Repackager or relabeler | accessdata.fda.gov |
| Rongeur | HTX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Saw, Manual And Accessories | GDR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Scoop | FHL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Screwdriver | HXX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Spatula, Surgical, General & Plastic Surgery | GAF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Specula, Ophthalmic | HNC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Speculum, Ent | EPY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Speculum, Rectal | FFQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Speculum, Vaginal, Metal | HDF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Spud, Ophthalmic | HNA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tray, Surgical | LRP | 1 | Repackager or relabeler | accessdata.fda.gov |
| Trephine, Manual, Ophthalmic | HRH | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tube, Tonsil Suction | KCB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Urethrotome | EZO | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|
| June 8, 2018 | K173070 | HSW Resection Instruments | HIH | Substantially Equivalent | Henke-Sass, Wolf GmbH | accessdata.fda.gov |
| December 7, 2017 | K171336 | Cystoscope 4.0mm autoclavable 0° WL 302mm; Hysteroscope 4.0mm autoclavable 0° WL 302mm; Cysto-Urethroscope Sheath 19 Fr.; Bridge for 17-25 Fr. Cysto-Urethroscope Sheath | FAJ | Substantially Equivalent | Henke-Sass, Wolf GmbH | accessdata.fda.gov |
| March 18, 2008 | K080560 | HENKE SASS WOLF OF AMERICA ARTHROSCOPE | HRX | Substantially Equivalent | Henke Sass Wolf of America, Inc. | accessdata.fda.gov |
| May 16, 1994 | K941541 | HSV LAPAROSCOPY SET | GCJ | Substantially Equivalent | Henke Sass Wolf of America, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 8, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.