Spire Medical, Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Spire Medical, Inc.” (first 1980, latest 1982), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 22 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| EQJ | Bur, Ear, Nose And Throat | 1 | 1 |
| ERL | Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | 1 | 1 |
| GFA | Blade, Saw, General & Plastic Surgery, Surgical | 1 | 1 |
| GFF | Bur, Surgical, General & Plastic Surgery | 1 | 1 |
| GFG | Bit, Surgical | 1 | 1 |
Review panels
Most recent Spire Medical, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K821487 | MICRO-SURGICAL POWER INSTRUMENT SYS. | GFA | 1982-07-02 | 45 |
| K821485 | DERMABRADERS | GFF | 1982-06-10 | 23 |
| K821486 | MICRO DRILLS | GFG | 1982-06-09 | 22 |
| K802503 | MICRO-SUGICAL POWER INSTRUMENT SYSTEM | EQJ | 1980-10-31 | 14 |
| K802463 | MICRO-SURGICAL POWER INSTRUMENT SYSTEM | ERL | 1980-10-31 | 22 |
Recalls
openFDA lists no recalls under a recalling firm named Spire Medical, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Spire Biomedical, Inc. (16 510(k)s)
- Spire, Inc. D/B/A Spire Health (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Spire Medical, Inc.?
FDA lists 5 510(k) clearances under the applicant name “Spire Medical, Inc.” (first 1980, latest 1982), across 5 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Spire Medical, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Spire Medical, Inc. is 22 days.
Which FDA product codes appear under Spire Medical, Inc.?
The most frequent FDA product codes under this applicant name are EQJ (Bur, Ear, Nose And Throat, 1); ERL (Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece, 1); GFA (Blade, Saw, General & Plastic Surgery, Surgical, 1).
Next steps
- See all 5 Spire Medical, Inc. clearances with predicates and recalls
- Run predicate analysis for product code EQJ, Spire Medical, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.