# Micromedics, Inc.

> Medical device manufacturer record on deviCERTS, compiled from public registries. Micromedics, Inc. is a medical device manufacturer based in the United States, with 221 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (EU Class IIa; FDA Class II, Class I and Unclassified) and 5 FDA recalls as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/micromedics-inc>
- Country: United States (from SRN)
- EUDAMED actor status: active
- Role: Manufacturer
- Registrations: EUDAMED, FDA
- EUDAMED SRN: US-MF-000018365
- FDA FEI: 2183425
- DUNS: 066839630

## Figures

- Devices: 221
- FDA recalls (matched to the firm by name): 5

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: FDA GUDID 154, EUDAMED 118, FDA 510(k) 28
- Device classes: EU Class IIa 118, FDA Class II 66, FDA Class I 34, FDA Unclassified 2
- EMDN [A02 Syringes](https://devicerts.com/categories/emdn/A02): 114 devices
- EMDN [A03 Tubular devices](https://devicerts.com/categories/emdn/A03): 4 devices

## Sites and related companies

- Authorised representative: [MDSS GmbH](https://devicerts.com/representatives/mdss-gmbh-de-ar-000005430) (Germany)

## Devices

The first 50 of 221, in the order of the canonical page, which lists them all.

- [Applicator Tip](https://devicerts.com/devices/applicator-tip-sa-3618) · ref SA-3618 · Class IIa · EUDAMED · status: Active
- [Instru-Safe Instrument Protection Systems](https://devicerts.com/devices/instru-safe-instrument-protection-systems-kct) · ref K051157 · Class II · 510(k) · status: Active · decision 2005-09-01
- [FibriJet](https://devicerts.com/devices/fibrijet-sa-3647-a058e0d6) · ref SA-3647 · Class IIa · EUDAMED · status: Active
- [FibriJet](https://devicerts.com/devices/fibrijet-sa-3671-f09a61c4) · ref SA-3671 · Class IIa · EUDAMED · status: Active
- [FibriJet](https://devicerts.com/devices/fibrijet-800-0251-827eb846) · ref 800-0251 · Class IIa · EUDAMED · status: Active
- [DuploTip](https://devicerts.com/devices/duplotip-0601137-0c9746b2) · ref 0601137 · Class IIa · EUDAMED · status: Active
- [Fibrijet SA-3668](https://devicerts.com/devices/fibrijet-sa-3668) · Class II · GUDID · status: Active
- [Biomet 800-0217](https://devicerts.com/devices/biomet-800-0217) · Class II · GUDID · status: Active
- [FibriJet SA-3646](https://devicerts.com/devices/fibrijet-sa-3646) · Class I · GUDID · status: Listed
- [Osteoprecision Gd-1015-100](https://devicerts.com/devices/osteoprecision-gd-1015-100) · Class II · GUDID · status: Active
- [Mitek Sports Medicine 278014](https://devicerts.com/devices/mitek-sports-medicine-278014) · Class I · GUDID · status: Listed
- [Pramand FS-2005](https://devicerts.com/devices/pramand-fs-2005) · Class II · GUDID · status: Listed
- [Fibrijet SA-3654](https://devicerts.com/devices/fibrijet-sa-3654) · Class II · GUDID · status: Active
- [FibriJet SA-3625](https://devicerts.com/devices/fibrijet-sa-3625) · Class I · GUDID · status: Listed
- [Duplotip SA374003000000](https://devicerts.com/devices/duplotip-sa374003000000) · Class II · GUDID · status: Active
- [Gasless Tip 601153](https://devicerts.com/devices/gasless-tip-601153) · Class II · GUDID · status: Active
- [FibriJet AMS700-B](https://devicerts.com/devices/fibrijet-ams700-b-bef559b6) · Class I · GUDID · status: Withdrawn
- [Fibrijet SA-6205](https://devicerts.com/devices/fibrijet-sa-6205) · Class II · GUDID · status: Listed
- [Baxter 0600128](https://devicerts.com/devices/baxter-0600128) · Class II · GUDID · status: Listed
- [Biomet Biologics 800-0211](https://devicerts.com/devices/biomet-biologics-800-0211) · Class I · GUDID · status: Listed
- [OsteoPrecision GD-1015-100-CC](https://devicerts.com/devices/osteoprecision-gd-1015-100-cc) · Class II · GUDID · status: Active
- [Fibrijet SA-3658](https://devicerts.com/devices/fibrijet-sa-3658) · Class II · GUDID · status: Active
- [FibriJet SA-6111](https://devicerts.com/devices/fibrijet-sa-6111) · Class II · GUDID · status: Listed
- [Osteoprecision Gd-1215-050](https://devicerts.com/devices/osteoprecision-gd-1215-050) · Class II · GUDID · status: Active
- [Baxter 0600225](https://devicerts.com/devices/baxter-0600225) · Class II · GUDID · status: Active
- [Duplotip 0600036](https://devicerts.com/devices/duplotip-0600036) · Class II · GUDID · status: Active
- [Gasless Tip 601155](https://devicerts.com/devices/gasless-tip-601155) · Class II · GUDID · status: Active
- [Fibrijet SA-3659](https://devicerts.com/devices/fibrijet-sa-3659) · Class II · GUDID · status: Active
- [Fibrijet SA-3664](https://devicerts.com/devices/fibrijet-sa-3664) · Class II · GUDID · status: Active
- [FibriJet SA-3610](https://devicerts.com/devices/fibrijet-sa-3610) · Class I · GUDID · status: Listed
- [Baxter 0601139](https://devicerts.com/devices/baxter-0601139) · Class II · GUDID · status: Active
- [Fibrijet SA-3868](https://devicerts.com/devices/fibrijet-sa-3868) · Class II · GUDID · status: Active
- [Osteoxpress Gd-5515](https://devicerts.com/devices/osteoxpress-gd-5515-e04212db) · Class II · GUDID · status: Active
- [Duplotip SA376003000000](https://devicerts.com/devices/duplotip-sa376003000000) · Class II · GUDID · status: Active
- [Celling Biosciences GDP Express Kit 0852-0001, CB-5515 and CB-3670](https://devicerts.com/devices/celling-biosciences-gdp-express-kit-0852-0001-cb-5515-an) · Class II · GUDID · status: Listed
- [Graft Delivery, DePuy Synthes 03-950-001S](https://devicerts.com/devices/graft-delivery-depuy-synthes-03-950-001s) · Class II · GUDID · status: Active
- [FibriJet AMS700-B](https://devicerts.com/devices/fibrijet-ams700-b) · Class I · GUDID · status: Listed
- [Celling Biosciences GDP Express Kit Component, CB-3670](https://devicerts.com/devices/celling-biosciences-gdp-express-kit-component-cb-3670-cb-3670) · Class II · GUDID · status: Listed
- [Duplotip SA375003000000](https://devicerts.com/devices/duplotip-sa375003000000) · Class II · GUDID · status: Active
- [App-100](https://devicerts.com/devices/na-app-100) · Class I · GUDID · status: Listed
- [HC Biologics HC-OPM100](https://devicerts.com/devices/hc-biologics-hc-opm100) · Class II · GUDID · status: Active
- [FibriJet SA-3627](https://devicerts.com/devices/fibrijet-sa-3627) · Class I · GUDID · status: Listed
- [Nordson Medical MA-1601](https://devicerts.com/devices/nordson-medical-ma-1601) · Class I · GUDID · status: Listed
- [Duplotip 0600038](https://devicerts.com/devices/duplotip-0600038) · Class II · GUDID · status: Active
- [FibriJet SA-3626](https://devicerts.com/devices/fibrijet-sa-3626) · Class I · GUDID · status: Listed
- [Fibrijet SA-3768](https://devicerts.com/devices/fibrijet-sa-3768) · Class II · GUDID · status: Active
- [Fibrijet SA-3657](https://devicerts.com/devices/fibrijet-sa-3657) · Class II · GUDID · status: Active
- [Nordson Medical PKG327](https://devicerts.com/devices/nordson-medical-pkg327) · Class II · GUDID · status: Active
- [FibriJet SA-3605](https://devicerts.com/devices/fibrijet-sa-3605) · Class I · GUDID · status: Listed
- [Osteoprecision Gd-1115-100](https://devicerts.com/devices/osteoprecision-gd-1115-100) · Class II · GUDID · status: Active

## FDA recalls (matched by name, newest first)

- Z-1817-2017 · Class II · Terminated · initiated 2016-10-20 · product code KGZ: The sterile packaging may contain small channels in the seal of the pouch, If the channels are present, the package integrity may be compromised which may affect sterility assurance.
- Z-0345-2011 · Unclassified (pre-2012) · Terminated · initiated 2010-03-15 · product code KYZ: Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.
- Z-0346-2011 · Unclassified (pre-2012) · Terminated · initiated 2010-03-15 · product code KYZ: Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches potentially resulting in a non-sterile product which may cause transmission of disease or infection.
- Z-0347-2011 · Unclassified (pre-2012) · Terminated · initiated 2010-03-15 · product code LFB: Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.
- Z-0348-2011 · Unclassified (pre-2012) · Terminated · initiated 2010-03-15 · product code ETD: Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.

## Source and citation

- Cite as: Micromedics, Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/micromedics-inc (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- EUDAMED record synced: 2026-11-07
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/micromedics-inc.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/manufacturers/micromedics-inc
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.