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Sign in to claim this brandTRINITY STERILE, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 201 Kiley Dr, SALISBURY, MD, 21801
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000123297
- DUNS Number
- —
Catalogue (390)
Page 4 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Trinity Sterile, Inc. | 85287SH | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | T97-810 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 10003 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 2280A | FDA UDI | N | Active |
| Trinity Sterile, Inc. | 7036 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50398 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 5006 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6001 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 22201 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 10005 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6022 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-805 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81360 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 82029 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5039 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5067 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50191 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50233 | FDA UDI | N/A | Active |
| Trinity Sterile, Inc. | 81451 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85387 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6023 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85287BWMC | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 7079 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85162 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20128 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | T98-817 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50857 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 20216 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5059 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5017 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81664 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20388 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 10048 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85377 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81428 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6092 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50771 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 20129 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | T97-934 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50666 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 22000 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5021 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 10006 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50195 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 6027 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50252 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 81254B | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7016 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7009 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50280 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (10)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Dec 13, 2024 | Z-1012-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1016-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1015-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1013-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1014-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Jun 29, 2022 | Z-1551-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1548-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1550-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1549-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Feb 23, 2021 | Z-1468-2021 | — | terminated | Evidence of face masks or other material in the seal in several kits, causing improper seals and compromised sterility |