# Groman Inc.

> Medical device manufacturer record on deviCERTS, compiled from public registries. Groman Inc. is a medical device manufacturer, with 22 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) and 1 FDA recall as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/groman-inc>
- Country: United States (from the FDA registration address)
- Role: Manufacturer
- Registrations: FDA
- FDA FEI: 3004361444
- DUNS: 020124663

## Figures

- Devices: 22
- FDA recalls (matched to the firm by name): 1

## Registry facts

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

- Registries: FDA GUDID 21, FDA 510(k) 1
- Device classes: FDA Class II 19, FDA Class I 3

## Devices

The first 22 of 22, in the order of the canonical page, which lists them all.

- [Etchmaster EM-L-N-RB](https://devicerts.com/devices/etchmaster-em-l-n-rb) · Class II · GUDID · status: Active
- [Etchmaster PM-X-L-RB](https://devicerts.com/devices/etchmaster-pm-x-l-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-S-O-RB](https://devicerts.com/devices/etchmaster-em-s-o-rb) · Class II · GUDID · status: Active
- [SafetyO2 AM-OXY-FP](https://devicerts.com/devices/safetyo2-am-oxy-fp) · Class I · GUDID · status: Listed
- [Etchmaster EM-S-K-RB](https://devicerts.com/devices/etchmaster-em-s-k-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-L-G-RB](https://devicerts.com/devices/etchmaster-em-l-g-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-L-K-CA](https://devicerts.com/devices/etchmaster-em-l-k-ca) · Class II · GUDID · status: Active
- [Etchmaster EM-L-K-RB](https://devicerts.com/devices/etchmaster-em-l-k-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-S-P-RB](https://devicerts.com/devices/etchmaster-em-s-p-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-L-Y-RB](https://devicerts.com/devices/etchmaster-em-l-y-rb) · Class II · GUDID · status: Active
- [SafetyFilta GRO-SF-NEB-25](https://devicerts.com/devices/safetyfilta-gro-sf-neb-25) · Class I · GUDID · status: Listed
- [SafetyNeb AM-NEB-FP](https://devicerts.com/devices/safetyneb-am-neb-fp) · Class I · GUDID · status: Listed
- [Etchmaster EM-S-R-RB](https://devicerts.com/devices/etchmaster-em-s-r-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-S-Y-RB](https://devicerts.com/devices/etchmaster-em-s-y-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-L-F-RB](https://devicerts.com/devices/etchmaster-em-l-f-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-S-K-CA](https://devicerts.com/devices/etchmaster-em-s-k-ca) · Class II · GUDID · status: Active
- [Etchmaster EM-L-R-RB](https://devicerts.com/devices/etchmaster-em-l-r-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-S-G-RB](https://devicerts.com/devices/etchmaster-em-s-g-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-L-B-RB](https://devicerts.com/devices/etchmaster-em-l-b-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-S-J-RB](https://devicerts.com/devices/etchmaster-em-s-j-rb) · Class II · GUDID · status: Active
- [Etchmaster EM-S-B-RB](https://devicerts.com/devices/etchmaster-em-s-b-rb) · Class II · GUDID · status: Active
- [Groman Prepmaster](https://devicerts.com/devices/groman-prepmaster-koj) · ref K030292 · Class II · 510(k) · status: Active · decision 2003-04-15

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

- Z-0742-2012 · Unclassified (pre-2012) · Terminated · initiated 2010-12-13 · product code KOJ: Groman Inc. of Margate, FL recalled their product Cordless Etcher Air Brush. When non-conforming cartridges are inserted into the Cordless Etcher they can induce excessive stresses on the device causing cracks in the plastic housing of the device. These crack can lead to a hazardous situation due to the high pressure of the gas contained in the CO2 cartridges.

## Source and citation

- Cite as: Groman Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/groman-inc (data as of 2026-11-15).
- Data sources: [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/)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/groman-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/groman-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.