Data / Medical devices / United States / Ferris MFG. Corp.
Ferris MFG. Corp.: FDA-registered device maker in Fort Worth, TX, United States, 8 510(k) clearances
Ferris MFG. Corp. is registered with the FDA (registration 1419520) in Fort Worth, TX, United States. It lists 7 device types. The FDA files 8 510(k) clearances under its listings, the newest dated February 22, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1419520
- Address
- 5133 Northeast Pkwy, Fort Worth, TX, United States, 76106
- Owner or operator
- FERRIS MFG. CORP. (1419520)
- Roles
- Manufacturer
- First device listed
- December 6, 2001
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Liquid | KMF | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic | MGQ | U | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Drug | FRO | U | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Occlusive | NAD | 1 | Manufacturer | accessdata.fda.gov |
| Nursing Pad, Polyurethane Pad With Starch Copolymer, Glycerin, And Surfactant (F-68) | NTX | 1 | Manufacturer | accessdata.fda.gov |
| Orthosis, Limb Brace | IQI | 1 | Manufacturer | accessdata.fda.gov |
| Orthosis, Lumbo-Sacral | IPY | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| February 22, 2005 | K031660 | FERRIS POLYMEM STERILE BREAST PAD | NTX | Substantially Equivalent | Ferris Mfg. Corp. | accessdata.fda.gov |
| October 22, 2003 | K031307 | FERRIS POLYMEM SILVER WOUND DRESSING | FRO | Substantially Equivalent | Ferris Mfg. Corp. | accessdata.fda.gov |
| August 27, 1999 | K991729 | FERRIS POLYOSTOMY STERILE WOUND DRESSING | KMF | Substantially Equivalent | Ferris Mfg. Corp. | accessdata.fda.gov |
| April 29, 1999 | K990906 | FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER | KMF | Substantially Equivalent for Some Indications | Ferris Mfg. Corp. | accessdata.fda.gov |
| September 22, 1998 | K982306 | POLYTUBE | MGQ | Substantially Equivalent | Ferris Mfg. Corp. | accessdata.fda.gov |
| June 7, 1994 | K932913 | FERRIS POLYMEM HYDROPHILIC WOUND DRESSING | KMF | Substantially Equivalent for Some Indications | Ferris Mfg. Corp. | accessdata.fda.gov |
| May 18, 1990 | K900127 | FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS) | KMF | Substantially Equivalent for Some Indications | Ferris Mfg. Corp. | accessdata.fda.gov |
| March 23, 1988 | K880330 | FERRIS HYDROPHILIC DRESSING | FRO | Substantially Equivalent for Some Indications | Ferris Mfg. Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Bandage, Liquid
- All makers of Orthosis, Lumbo-Sacral
- All makers of Dressing, Wound, Drug
- All makers of Orthosis, Limb Brace
- All makers of Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
- All makers of Dressing, Wound, Occlusive
Updated February 22, 2005. 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.