Data / Medical devices / United States / Htl-Strefa, Inc.
Htl-Strefa, Inc.: FDA-registered device maker in Woodstock, GA, United States, 22 510(k) clearances
Htl-Strefa, Inc. is registered with the FDA (registration 3006142663) in Woodstock, GA, United States. It lists 7 device types. The FDA files 22 510(k) clearances under its listings, the newest dated July 1, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3006142663
- Address
- 113 Towne Lake Pkwy Ste 120, Woodstock, GA, United States, 30188
- Owner or operator
- HTL-STREFA S.A. (9028458)
- Roles
- Complaint file establishment
- First device listed
- October 31, 1996
- Registered through
- 2027
- Brand names listed
- Acti-Lance, Acti-Lance baby, Artsana Insulin Syringes, Clickfine pen needles, DropSafe Acti-Lance Safety Lancets, DropSafe Haemolance Plus Safety Lancets, DropSafe MediSafe Solo Safety Lancets, DropSafe Medlance Plus Safety Lancets and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | 2 | Complaint file establishment | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Complaint file establishment | accessdata.fda.gov |
| Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FMK | 2 | Complaint file establishment | accessdata.fda.gov |
| Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature | QRK | 2 | Complaint file establishment | accessdata.fda.gov |
| Syringe, Antistick | MEG | 2 | Complaint file establishment | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Complaint file establishment | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| July 1, 2025 | K250016 | droplet® personal lancets | QRK | Substantially Equivalent | Htl-Strefa S.A | accessdata.fda.gov |
| January 20, 2023 | K203792 | Insupen Pen needle, Insupen ORIGINAL Pen Needle, Insupen ADVANCED pen needle | FMI | Substantially Equivalent | Pikdare Spa | accessdata.fda.gov |
| December 2, 2022 | K223353 | DropSafeTM SicuraTM | FMI | Substantially Equivalent | Pikdare Spa | accessdata.fda.gov |
| July 8, 2022 | K220643 | DropSafe Acti-Lance Safety Lancets; droplet ACTI-LANCE Safety Lancets, DropSafe Medlance Plus Safety Lancets; droplet MEDLANCE PLUS Safety Lancets, DropSafe ergoLance Safety Lancets, DropSafe Prolance Safety Lancets, DropSafe Medisafe Solo Safety Lancets; DropSafe Haemolance Plus Safety Lancets | FMK | Substantially Equivalent | Htl-Strefa S.A | accessdata.fda.gov |
| January 18, 2022 | K201044 | CHIRANA Insulin Syringes | FMF | Substantially Equivalent | Chirana T. Injecta | accessdata.fda.gov |
| January 7, 2022 | K211716 | DropSafe Safety Pen Needles | FMI | Substantially Equivalent | Htl Strefa SA | accessdata.fda.gov |
| October 15, 2020 | K202340 | Droplet Pen Needle 30G & 33G | FMI | Substantially Equivalent | Htl-Strefa S.A | accessdata.fda.gov |
| April 21, 2020 | K192082 | Droplet Pen Needle 34G | FMI | Substantially Equivalent | Htl-Strefa S.A | accessdata.fda.gov |
| May 11, 2018 | K180385 | Infrared Body Thermometer | FLL | Substantially Equivalent | Hetaida Technology Co., Ltd. | accessdata.fda.gov |
| March 21, 2018 | K171982 | DROPLET PEN NEEDLE | FMI | Substantially Equivalent | Htl-Strefa S.A | accessdata.fda.gov |
| December 12, 2017 | K170988 | DropSafe Safety Pen Needle | FMI | Substantially Equivalent | Htl-Strefa S.A | accessdata.fda.gov |
| October 11, 2017 | K171984 | Clickfine Pen Needle, Penfine Classic Pen Needle | FMI | Substantially Equivalent | Ypsomed AG | accessdata.fda.gov |
| August 2, 2017 | K170651 | Sterile Disposable Syringe with Safety Needle, Sterile Disposable Syringe with Needle, Sterile Disposable Syringe, Sterile Disposable Safety Needle, Sterile Disposable Needle | MEG | Substantially Equivalent | Yangzhou Medline Industry, Co., Ltd. | accessdata.fda.gov |
| June 17, 2016 | K153537 | Sol-M Insulin Syringe, Sol-M TB Syringe | FMF | Substantially Equivalent | Sol-Millennium Medical, Inc. | accessdata.fda.gov |
| May 12, 2016 | K153670 | Genteel Lancing Device | FMK | Substantially Equivalent | Genteel, LLC | accessdata.fda.gov |
| February 10, 2016 | K151311 | Safe Block Pen Needle | FMI | Substantially Equivalent | Artsana S.P.A | accessdata.fda.gov |
| June 25, 2015 | K143437 | Droplet Pen Needles | FMI | Substantially Equivalent | Htl-Strefa S.A | accessdata.fda.gov |
| May 22, 2014 | K132681 | SOL-GUARD INSULIN AND TUBERCULIN SAFETY SYRINGE | MEG | Substantially Equivalent | Sol-Millennium Medical, Inc. | accessdata.fda.gov |
| May 8, 2013 | K123684 | SOL-CARE SAFETY NEEDLE | FMI | Substantially Equivalent | Sol-Millennium Medical | accessdata.fda.gov |
| August 20, 2010 | K101359 | INVIROSTRIPE LUER LOCK SYRINGES (1, 3, 10, 20, 30 AND 60 ML) | FMF | Substantially Equivalent | Inviro Medical Devices, Inc. | accessdata.fda.gov |
| November 25, 2005 | K052667 | ARTSANA PISTON AND INSULIN SYRINGES | FMF | Substantially Equivalent | Artsana S.P.A | accessdata.fda.gov |
| October 4, 2005 | K051783 | ARTSANA PEN NEEDLES, ARTSANA INJECTION NEEDLES | FMI | Substantially Equivalent | Artsana S.P.A | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Piston
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Syringe, Antistick
- All makers of Tape And Bandage, Adhesive
- All makers of Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- All makers of Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature
Updated July 1, 2025. 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.